A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3007n100



Internal ID20154623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69994778..70164481hg38UCSC Ensembl
chr16:70028681..70198384hg19UCSC Ensembl
chr16:68586182..68755885hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38169704
hg19169704
hg18169704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059728, nsv1064405, nsv1065118, nsv1063731
Samples
Known GenesMIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3007n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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